CDC-Authored Genomics and Precision Health Publications Database
Last data update: Jan 13, 2025. (Total: 6490 publications)
Query Trace: Lockhart ER[original query] |
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Challenges and opportunities for integrating genetic testing into a diagnostic workflow: heritable long QT syndrome as a model.
Lubin IM , Lockhart ER , Frank J , See VY , Vashist S , Greene C . Diagnosis (Berl) 2019 8 (1) 17-26 |
Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings.
Lubin IM , Aziz N , Babb LJ , Ballinger D , Bisht H , Church DM , Cordes S , Eilbeck K , Hyland F , Kalman L , Landrum M , Lockhart ER , Maglott D , Marth G , Pfeifer JD , Rehm HL , Roy S , Tezak Z , Truty R , Ullman-Cullere M , Voelkerding KV , Worthey E , Zaranek AW , Zook JM . J Mol Diagn 2017 19 (3) 417-426 |
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